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Watching DNA polymerase η make a phosphodiester bond

Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are ali...

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Autores principales: Nakamura, Teruya, Zhao, Ye, Yamagata, Yuriko, Hua, Yue-jin, Yang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397672/
https://www.ncbi.nlm.nih.gov/pubmed/22785315
http://dx.doi.org/10.1038/nature11181
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author Nakamura, Teruya
Zhao, Ye
Yamagata, Yuriko
Hua, Yue-jin
Yang, Wei
author_facet Nakamura, Teruya
Zhao, Ye
Yamagata, Yuriko
Hua, Yue-jin
Yang, Wei
author_sort Nakamura, Teruya
collection PubMed
description Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are aligned for reaction within 40 seconds, but the new bond begins to form at 80 seconds. Structures at reaction times from 80s to 300s reveal a mixture of decreasing substrate and increasing product of the nucleotidyl-transfer reaction. In sequence, the nucleophile 3′-OH is deprotonated, the deoxyribose at the primer end converts from C2′-endo to C3′-endo to avoid steric clashes, and the nucleophile and the α-phosphate of dATP approach each other to form the new bond. A third Mg(2+) ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism.
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spelling pubmed-33976722013-01-12 Watching DNA polymerase η make a phosphodiester bond Nakamura, Teruya Zhao, Ye Yamagata, Yuriko Hua, Yue-jin Yang, Wei Nature Article Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are aligned for reaction within 40 seconds, but the new bond begins to form at 80 seconds. Structures at reaction times from 80s to 300s reveal a mixture of decreasing substrate and increasing product of the nucleotidyl-transfer reaction. In sequence, the nucleophile 3′-OH is deprotonated, the deoxyribose at the primer end converts from C2′-endo to C3′-endo to avoid steric clashes, and the nucleophile and the α-phosphate of dATP approach each other to form the new bond. A third Mg(2+) ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism. 2012-07-11 /pmc/articles/PMC3397672/ /pubmed/22785315 http://dx.doi.org/10.1038/nature11181 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Nakamura, Teruya
Zhao, Ye
Yamagata, Yuriko
Hua, Yue-jin
Yang, Wei
Watching DNA polymerase η make a phosphodiester bond
title Watching DNA polymerase η make a phosphodiester bond
title_full Watching DNA polymerase η make a phosphodiester bond
title_fullStr Watching DNA polymerase η make a phosphodiester bond
title_full_unstemmed Watching DNA polymerase η make a phosphodiester bond
title_short Watching DNA polymerase η make a phosphodiester bond
title_sort watching dna polymerase η make a phosphodiester bond
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397672/
https://www.ncbi.nlm.nih.gov/pubmed/22785315
http://dx.doi.org/10.1038/nature11181
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